400 related articles for article (PubMed ID: 9504785)
1. Unusual features in children with inv dup(15) supernumerary marker: a study of genotype-phenotype correlation in Taiwan.
Hou JW; Wang TR
Eur J Pediatr; 1998 Feb; 157(2):122-7. PubMed ID: 9504785
[TBL] [Abstract][Full Text] [Related]
2. The inv dup (15) or idic (15) syndrome (Tetrasomy 15q).
Battaglia A
Orphanet J Rare Dis; 2008 Nov; 3():30. PubMed ID: 19019226
[TBL] [Abstract][Full Text] [Related]
3. Triplication of 15q11-q13 with inv dup(15) in a female with developmental delay.
Long FL; Duckett DP; Billam LJ; Williams DK; Crolla JA
J Med Genet; 1998 May; 35(5):425-8. PubMed ID: 9610809
[TBL] [Abstract][Full Text] [Related]
4. Molecular cytogenetic characterization of an inv dup(15) chromosome presenting as a small supernumerary marker chromosome associated with the inv dup(15) syndrome.
Chen CP; Lin SP; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Town DD; Yang CW; Wang W
Taiwan J Obstet Gynecol; 2016 Oct; 55(5):728-732. PubMed ID: 27751425
[TBL] [Abstract][Full Text] [Related]
5. Simultaneous formation of inv dup(15) and dup(15q) in a girl with developmental delay: origin of the abnormal chromosomes.
Abeliovich D; Dagan J; Werner M; Lerer I; Shapira Y; Meiner V
Eur J Hum Genet; 1995; 3(1):49-55. PubMed ID: 7767656
[TBL] [Abstract][Full Text] [Related]
6. Supernumerary inv dup(15) in a patient with Angelman syndrome and a deletion of 15q11-q13.
Spinner NB; Zackai E; Cheng SD; Knoll JH
Am J Med Genet; 1995 May; 57(1):61-5. PubMed ID: 7645601
[TBL] [Abstract][Full Text] [Related]
7. Cytogenetic and molecular characterization of inverted duplicated chromosomes 15 from 11 patients.
Cheng SD; Spinner NB; Zackai EH; Knoll JH
Am J Hum Genet; 1994 Oct; 55(4):753-9. PubMed ID: 7942854
[TBL] [Abstract][Full Text] [Related]
8. Refined molecular characterization of the breakpoints in small inv dup(15) chromosomes.
Huang B; Crolla JA; Christian SL; Wolf-Ledbetter ME; Macha ME; Papenhausen PN; Ledbetter DH
Hum Genet; 1997 Jan; 99(1):11-7. PubMed ID: 9003485
[TBL] [Abstract][Full Text] [Related]
9. Clinical and molecular analysis of five inv dup(15) patients.
Robinson WP; Binkert F; Giné R; Vazquez C; Müller W; Rosenkranz W; Schinzel A
Eur J Hum Genet; 1993; 1(1):37-50. PubMed ID: 8069650
[TBL] [Abstract][Full Text] [Related]
10. The inv dup(15) syndrome: a clinically recognizable syndrome with altered behavior, mental retardation, and epilepsy.
Battaglia A; Gurrieri F; Bertini E; Bellacosa A; Pomponi MG; Paravatou-Petsotas M; Mazza S; Neri G
Neurology; 1997 Apr; 48(4):1081-6. PubMed ID: 9109904
[TBL] [Abstract][Full Text] [Related]
11. Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization.
Blennow E; Nielsen KB; Telenius H; Carter NP; Kristoffersson U; Holmberg E; Gillberg C; Nordenskjöld M
Am J Med Genet; 1995 Jan; 55(1):85-94. PubMed ID: 7702104
[TBL] [Abstract][Full Text] [Related]
12. A clinical, cytogenetic and molecular study of ten probands with supernumerary inv dup (15) marker chromosomes.
Webb T; Hardy CA; King M; Watkiss E; Mitchell C; Cole T
Clin Genet; 1998 Jan; 53(1):34-43. PubMed ID: 9550359
[TBL] [Abstract][Full Text] [Related]
13. The inv dup(15) or idic(15) syndrome: a clinically recognisable neurogenetic disorder.
Battaglia A
Brain Dev; 2005 Aug; 27(5):365-9. PubMed ID: 16023554
[TBL] [Abstract][Full Text] [Related]
14. Cytogenetic and molecular analysis of inv dup(15) chromosomes observed in two patients with autistic disorder and mental retardation.
Flejter WL; Bennett-Baker PE; Ghaziuddin M; McDonald M; Sheldon S; Gorski JL
Am J Med Genet; 1996 Jan; 61(2):182-7. PubMed ID: 8669450
[TBL] [Abstract][Full Text] [Related]
15. Uniparental disomy explains the occurrence of the Angelman or Prader-Willi syndrome in patients with an additional small inv dup(15) chromosome.
Robinson WP; Wagstaff J; Bernasconi F; Baccichetti C; Artifoni L; Franzoni E; Suslak L; Shih LY; Aviv H; Schinzel AA
J Med Genet; 1993 Sep; 30(9):756-60. PubMed ID: 8411071
[TBL] [Abstract][Full Text] [Related]
16. Molecular characterisation of four cases of intrachromosomal triplication of chromosome 15q11-q14.
Ungaro P; Christian SL; Fantes JA; Mutirangura A; Black S; Reynolds J; Malcolm S; Dobyns WB; Ledbetter DH
J Med Genet; 2001 Jan; 38(1):26-34. PubMed ID: 11134237
[TBL] [Abstract][Full Text] [Related]
17. Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: clinical implications.
Leana-Cox J; Jenkins L; Palmer CG; Plattner R; Sheppard L; Flejter WL; Zackowski J; Tsien F; Schwartz S
Am J Hum Genet; 1994 May; 54(5):748-56. PubMed ID: 8178816
[TBL] [Abstract][Full Text] [Related]
18. Inv dup(15) supernumerary marker chromosomes.
Webb T
J Med Genet; 1994 Aug; 31(8):585-94. PubMed ID: 7815414
[No Abstract] [Full Text] [Related]
19. Mild generalized epilepsy and developmental disorder associated with large inv dup(15).
Chifari R; Guerrini R; Pierluigi M; Cavani S; Sgrò V; Elia M; Canger R; Canevini MP
Epilepsia; 2002 Sep; 43(9):1096-100. PubMed ID: 12199736
[TBL] [Abstract][Full Text] [Related]
20. Partial hexasomy of chromosome 15.
Huang B; Bartley J
Am J Med Genet A; 2003 Sep; 121A(3):277-80. PubMed ID: 12923871
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]